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首页> 外文期刊>Microbial drug resistance: MDR : Mechanisms, epidemiology, and disease >In Vitro Synergistic Activity of Colistin and Ceftazidime or Ciprofloxacin Against Multidrug-Resistant Clinical Strains of Pseudomonas aeruginosa
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In Vitro Synergistic Activity of Colistin and Ceftazidime or Ciprofloxacin Against Multidrug-Resistant Clinical Strains of Pseudomonas aeruginosa

机译:Colistin和头孢他啶或环丙沙星对铜绿假单胞菌多药耐药临床菌株的体外协同活性

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Infections caused by multidrug resistant (MDR) Pseudomonas aeruginosa are difficult to treat. Antibiotic development is dwindling in recent years. In order to develop new alternate therapies antimicrobial activity of different antibiotic combinations are being studied in vitro and in vivo. Sub-inhibitory concentrations of colistin were tested in combination with ceftazidime or ciprofloxacin by the checkerboard method against 25 MDR strains of P. aeruginosa. Synergy was observed for ceftazidime or ciprofloxacin antibiotic combinations with colistin among 73.3% of MDR3 (R-AMK,R- GEN,R- TOB R-CAZ R-CIP) strains and 100% of MDR4 (R-AMK,R- GEN,R- TOB R-CAZ R-CIP R-TZP) strains. 6.6% strains of MDR3 and 14.3% strains of MDR5 (R-AMK,R- GEN,R- TOB R-CAZ R-CIP R-TZP R-IPM) phenotypes were inhibited by colistin and ceftazidime alone and 6.6% strains of MDR3 phenotypes were inhibited by colistin and ciprofloxacin alone. For the remaining strains, though synergy was not observed, significant reduction in minimum inhibitory concentration was evident. The results of this study are significant as sub-inhibitory concentrations of colistin have an advantage of reducing in vivo toxicity. These findings need further evaluation for clinical use.
机译:由多药耐药性(MDR)的铜绿假单胞菌引起的感染很难治疗。近年来,抗生素的开发正在减少。为了开发新的替代疗法,正在体外和体内研究不同抗生素组合的抗微生物活性。通过棋盘法对25种铜绿假单胞菌MDR菌株与头孢他啶或环丙沙星联合测试了大肠菌素的亚抑制浓度。在73.3%的MDR3(R-AMK,R-GEN,R-TOB R-CAZ R-CIP)菌株和100%的MDR4(R-AMK,R-GEN,)菌株中观察到头孢他啶或环丙沙星抗生素与粘菌素的协同作用。 R-TOB R-CAZ R-CIP R-TZP)菌株。表型分别被粘菌素和头孢他啶抑制了6.6%的MDR3菌株和14.3%的MDR5(R-AMK,R-GEN,R-TOB R-CAZ R-CIP R-TZP R-IPM)表型和6.6%的MDR3菌株表型被粘菌素和环丙沙星单独抑制。对于其余菌株,尽管未观察到协同作用,但最低抑菌浓度明显降低。这项研究的结果非常重要,因为粘菌素的亚抑制浓度具有降低体内毒性的优势。这些发现需要进一步评估以用于临床。

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